22 results · 32ms · Sources: EU EUDAMED, US FDA

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FORTIFY ASSURA DR ICD, US

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·June 13, 2016

FORTIFY ASSURA VR ICD_IDE_US

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

ELLIPSE VR ICD

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017

CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017

SMALL PERIPHERAL CUTTING BALLOON

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NWX·August 19, 2019

FORTIFY ASSURA VR ICD_IDE_US

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017

UNIFY ASSURA CRT-D RF HV

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 29, 2019

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·January 11, 2013

8800

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·November 10, 2010

PINN CAN BONE SCREW 6.5MMX25MM

FDA Adverse Event
Injury ·JOHNSON & JOHNSON MEDICAL(SUZHOU)LTD.3006356043·Product code NDJ·July 2, 2014

FORTIFY ST DR, U1.6 SJ4 ID

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017

FORTIFYASSURA DR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017

FORTIFY ASSURA VR ICD_O_US

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 27, 2016

SMALL PERIPHERAL CUTTING BALLOON

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LOX·May 5, 2011

COMPREHENSIVE REVERSE SHOULDER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code PAO·December 30, 2016

COMPREHENSIVE REVERSE SHOULDER-MINI BASEPLATE

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·December 30, 2016

COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW 3.5MM HEX 4.75 X1 5MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·September 21, 2016

COMPREHENSIVE REVERE SHOULDER FIXED LOCKING SCREW 3.5MM HEX 4.75 X 20MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·September 21, 2016

COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW 6.5MM X 35MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·September 21, 2016

COMP LK SCR 3.5HEX 4.75X15 ST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 1, 2018